Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.46875806C>T | CA199514 | LRP4 | c.3697G>A (p.Glu1233Lys) c.3910G>A (p.Glu1304Lys) c.2893G>A (p.Glu965Lys) c.1462G>A (p.Glu488Lys) | ClinVar dbSNP gnomAD v4 |
11 | g.46875806C= | CA1969122432 | LRP4 | c.3697G= (p.Glu1233=) c.3910G= (p.Glu1304=) c.2893G= (p.Glu965=) c.1462G= (p.Glu488=) | dbSNP |